A curated catalogue of human genomic structural variation

Variant Details

Variant: dgv122e214

Internal ID20121545
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46274728..46325913hg38UCSC Ensembl
chr10:47645964..47697149hg19UCSC Ensembl
Allele length
AssemblyAllele length
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3623135, esv3623134
SamplesHG01878, NA20903, HG03135, HG02477, NA20787, HG03760, NA18951, NA19321, NA20890, NA12342, NA07056, HG01205, HG00731, HG01444, HG03055, HG03129, HG01506, NA18550, HG01098, HG02450, NA18948, NA12813, HG00117, NA19338, HG01537, HG02508, HG01131, NA18546, NA21135, HG02471, HG01708, HG03103, HG03585, HG01344, HG01461, HG03548, HG03538, HG00177, HG04094, HG03796, NA20798, NA20803, HG04106, HG00188, HG03863, HG00353, NA18868, HG00290, HG04076, HG00244, HG02836, NA18934, NA19239, HG04188, HG02696, HG01672, NA18957, HG00096, NA20757, HG01122, HG03686, NA20908, HG01398, HG02861, HG03787, HG04194, NA12273, HG00315, NA07048, NA19351, HG03464, NA18959, NA21116, HG01360, NA20520, HG00254, HG00982, HG01628, HG00343, NA19324, HG02224, HG02757, HG00742, NA12046, HG01465, NA19771, HG02019, HG01413, HG02054, HG00360, HG03209, NA12778, HG03660, HG03753, NA12275, HG01121, HG02807, HG02501, HG01676, NA19707, HG02586, NA19141, HG03132, HG03385, NA18543, NA18940, HG00109, HG02309, NA10851, HG03691, HG03237, HG04155, NA19794, HG01405, NA12749, HG01695, NA20799, HG01632, HG01269, HG03694, NA19747, NA20318, HG01669, HG03105, NA20507, NA20317, HG01485, HG01783, HG03259, HG03139, HG01791, NA20904, HG03515, HG02051, HG01890, HG00271, HG00278, HG02095, HG03490, HG00531, HG01354, NA19922
Known GenesANTXRL
PlatformMultiple platforms
Pubmed ID21293372
Accession Number(s)dgv122e214
Sample Size2504
Observed Gain142
Observed Loss0
Observed Complex0

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